RESUMEN
Different generations of polyamidoamine dendrimers were synthesized on a focal core of magnetic graphene oxide modified with 3-aminopropyltriethoxysilane. After the characterization of synthesized dendrimers, its second generation was employed as a suitable sorbent for simultaneous separation/preconcentration of diclofenac and acetaminophen by a dispersive magnetic solid phase microextraction. The extracted analytes were then quantified by high-performance liquid chromatography with ultraviolet detection. Under optimized conditions, the limits of detection were 0.3 µg/L for diclofenac and 0.1 µg/L for acetaminophen. The intra-day relative standard deviations at 50 µg L-1 levels were 1.8% for diclofenac and 2.1% for acetaminophen, while the inter-day relative standard deviations were 3.6% and 4.5% for diclofenac and acetaminophen, respectively. The calibration graphs were linear in ranges of 1.0-500.0 µg/L and 0.5-600.0 µg/L for diclofenac and acetaminophen, respectively, with good coefficients of determination (r2 > 0.998). The method was successfully applied to the determination of diclofenac and acetaminophen in water, milk, and biological samples.
Asunto(s)
Dendrímeros , Microextracción en Fase Líquida , Diclofenaco , Acetaminofén , Cromatografía Líquida de Alta Presión , Fenómenos Magnéticos , Microextracción en Fase Líquida/métodos , Extracción en Fase Sólida/métodosRESUMEN
A novel dispersive magnetic solid phase microextraction method based on ionic liquid-coated and cyclodextrin-functionalized magnetic core dendrimer nanocomposites has been developed for the determination of pyrethroids in juice samples. The different generation magnetic core dendrimer nanocomposites were successfully synthesized and the nanocomposites possess both the selective retention of guest dendrimer and cyclodextrin molecules and high adsorption capacities of ionic liquids. The extraction efficiencies of different generation magnetic core dendrimer nanocomposites were compared, and the type of nanocomposite with the highest recovery was obtained. Under the optimized experimental conditions, the method showed good linearity in the range of 3.5-500⯵gâ¯L-1. The LODs and LOQs were in the ranges of 0.36-1.3⯵gâ¯L-1 and 1.2-4.3⯵gâ¯L-1, respectively. The method also showed acceptable accuracies ranging from 98.2% to 99.4%. The proposed method was demonstrated to broaden the potential applications of dendrimer for the detection of pyrethroid residues in various juice samples.
Asunto(s)
Jugos de Frutas y Vegetales/análisis , Líquidos Iónicos/química , Piretrinas/química , Microextracción en Fase Sólida/métodos , Cromatografía Líquida de Alta Presión , Ciclodextrinas , Dendrímeros/química , Nanocompuestos , Piretrinas/aislamiento & purificaciónRESUMEN
Ternary deep eutectic solvent magnetic molecularly imprinted polymers grafted on silica were developed for the selective recognition and separation of theophylline, theobromine, (+)-catechin hydrate, and caffeic acid from green tea through dispersive magnetic solid-phase microextraction. A new ternary deep eutectic solvent was adopted as a functional monomer. The materials obtained were characterized by FTIR spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, NMR spectroscopy, and powder X-ray diffraction. The practical recovery of the theophylline, theobromine, (+)-catechin hydrate, and caffeic acid isolated with ternary deep eutectic solvent magnetic molecularly imprinted polymers in green tea were 91.82, 92.13, 89.96, and 90.73%, respectively, and the actual amounts extracted were 5.82, 4.32, 18.36, and 3.69 mg/g, respectively. The new method involving the novel material coupled with dispersive magnetic solid-phase microextraction showed outstanding recognition, selectivity and excellent magnetism, providing a new perspective for the separation of bioactive compounds.